A New Genetic Insight for Orphan Renal Disorder, Fabry: A Review
Pragati Karemore, Dinesh Kumar & Anil Kumar · Journal of Pharmaceutical Research International · 2021
Fabry is the rare X-linked genetic disorder caused due to mutation in Alpha –Galactosidase encoding GLA gene mutation in chromosome number 22. It has wide diversification in prevalence due to clinical heterozygosity. There are some potential biomarkers for the evaluation of norma...
Open access
Research Article
10.9734/jpri/2021/v33i58A34152